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- source_evidence_literature type ECO_0000212 NP853169.RAeuS-0Z1hxRmpTIPd81iA6j8_s7TmMxaXOk1eV0eMvkg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP853169.RAeuS-0Z1hxRmpTIPd81iA6j8_s7TmMxaXOk1eV0eMvkg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP853169.RAeuS-0Z1hxRmpTIPd81iA6j8_s7TmMxaXOk1eV0eMvkg130_provenance.
- NP853169.RAeuS-0Z1hxRmpTIPd81iA6j8_s7TmMxaXOk1eV0eMvkg130_assertion description "[In order to identify recurrent chromosomal regions of gain and loss, as well as novel gene targets of potential importance for MFH development and/or progression, we have analysed DNA copy number changes in 33 MFHs using microarray-based comparative genomic hybridisation (array CGH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP853169.RAeuS-0Z1hxRmpTIPd81iA6j8_s7TmMxaXOk1eV0eMvkg130_provenance.
- NP853169.RAeuS-0Z1hxRmpTIPd81iA6j8_s7TmMxaXOk1eV0eMvkg130_assertion evidence source_evidence_literature NP853169.RAeuS-0Z1hxRmpTIPd81iA6j8_s7TmMxaXOk1eV0eMvkg130_provenance.
- NP853169.RAeuS-0Z1hxRmpTIPd81iA6j8_s7TmMxaXOk1eV0eMvkg130_assertion SIO_000772 21085701 NP853169.RAeuS-0Z1hxRmpTIPd81iA6j8_s7TmMxaXOk1eV0eMvkg130_provenance.
- NP853169.RAeuS-0Z1hxRmpTIPd81iA6j8_s7TmMxaXOk1eV0eMvkg130_assertion wasDerivedFrom befree-2016 NP853169.RAeuS-0Z1hxRmpTIPd81iA6j8_s7TmMxaXOk1eV0eMvkg130_provenance.
- NP853169.RAeuS-0Z1hxRmpTIPd81iA6j8_s7TmMxaXOk1eV0eMvkg130_assertion wasGeneratedBy ECO_0000203 NP853169.RAeuS-0Z1hxRmpTIPd81iA6j8_s7TmMxaXOk1eV0eMvkg130_provenance.
- befree-2016 importedOn "2016-02-19" NP853169.RAeuS-0Z1hxRmpTIPd81iA6j8_s7TmMxaXOk1eV0eMvkg130_provenance.